21-(Furan-2-yl)henicosa-14,16-diyn-1-ol

Details

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Internal ID ea252e62-b23e-44d1-9ff5-f35c91c9e7ab
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 21-(furan-2-yl)henicosa-14,16-diyn-1-ol
SMILES (Canonical) C1=COC(=C1)CCCCC#CC#CCCCCCCCCCCCCCO
SMILES (Isomeric) C1=COC(=C1)CCCCC#CC#CCCCCCCCCCCCCCO
InChI InChI=1S/C25H38O2/c26-23-19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-21-25-22-20-24-27-25/h20,22,24,26H,1-5,7,9,11,13-19,21,23H2
InChI Key ASJAOJGETFTZHI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H38O2
Molecular Weight 370.60 g/mol
Exact Mass 370.287180451 g/mol
Topological Polar Surface Area (TPSA) 33.40 Ų
XlogP 8.50
Atomic LogP (AlogP) 6.67
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 21-(Furan-2-yl)henicosa-14,16-diyn-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 - 0.7176 71.76%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6030 60.30%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8850 88.50%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7740 77.40%
P-glycoprotein inhibitior - 0.6717 67.17%
P-glycoprotein substrate - 0.9052 90.52%
CYP3A4 substrate - 0.5668 56.68%
CYP2C9 substrate - 0.8005 80.05%
CYP2D6 substrate - 0.7090 70.90%
CYP3A4 inhibition - 0.9342 93.42%
CYP2C9 inhibition - 0.6778 67.78%
CYP2C19 inhibition - 0.6328 63.28%
CYP2D6 inhibition - 0.8870 88.70%
CYP1A2 inhibition - 0.7386 73.86%
CYP2C8 inhibition - 0.5740 57.40%
CYP inhibitory promiscuity - 0.7513 75.13%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Danger 0.5000 50.00%
Eye corrosion - 0.6897 68.97%
Eye irritation + 0.6041 60.41%
Skin irritation + 0.6710 67.10%
Skin corrosion - 0.5987 59.87%
Ames mutagenesis - 0.6854 68.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6840 68.40%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5226 52.26%
skin sensitisation - 0.6667 66.67%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6018 60.18%
Acute Oral Toxicity (c) III 0.5842 58.42%
Estrogen receptor binding + 0.7460 74.60%
Androgen receptor binding - 0.5797 57.97%
Thyroid receptor binding + 0.6700 67.00%
Glucocorticoid receptor binding - 0.4845 48.45%
Aromatase binding - 0.5254 52.54%
PPAR gamma + 0.7453 74.53%
Honey bee toxicity - 0.9516 95.16%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6756 67.56%
Fish aquatic toxicity - 0.8179 81.79%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.47% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.16% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.75% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.86% 86.33%
CHEMBL2581 P07339 Cathepsin D 83.65% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.31% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 81.39% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Polyalthia evecta

Cross-Links

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PubChem 11639293
LOTUS LTS0053617
wikiData Q104917869